proline and Batten Turner Congenital Myopathy

proline has been researched along with Batten Turner Congenital Myopathy in 2 studies

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's1 (50.00)18.2507
2000's1 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chang, LI; Chen, PR; Hsiao, KM; Jou, SB; Pan, H1
Dubowitz, V; Lehmann-Horn, F; Lerche, H; Mitrovic, N1

Other Studies

2 other study(ies) available for proline and Batten Turner Congenital Myopathy

ArticleYear
Novel CLCN1 mutations in Taiwanese patients with myotonia congenita.
    Journal of neurology, 2004, Volume: 251, Issue:6

    Topics: Adolescent; Adult; Aspartic Acid; Child; Chloride Channels; DNA Mutational Analysis; Female; Glycine; Humans; Isoleucine; Male; Mutation, Missense; Myotonia Congenita; Phenylalanine; Polymorphism, Genetic; Proline; Serine; Taiwan; Threonine

2004
Paramyotonia congenita: the R1448P Na+ channel mutation in adult human skeletal muscle.
    Annals of neurology, 1996, Volume: 39, Issue:5

    Topics: Adult; Arginine; Biopsy; Cold Temperature; Female; Hot Temperature; Humans; Ion Channel Gating; Isometric Contraction; Microelectrodes; Muscle Weakness; Muscle, Skeletal; Myotonia Congenita; Patch-Clamp Techniques; Point Mutation; Proline; Sodium Channels; Walking

1996